Canonical Allele Identifier: CA103120437
Gene:

Linked Data

dbSNP Id: rs1043639617
gnomAD v4: 4-102501037-A-G
MyVariant Identifiers: chr4:g.103422194A>G (hg19) chr4:g.102501037A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501037A>G , CM000666.2:g.102501037A>G GRCh38
NC_000004.11:g.103422194A>G , CM000666.1:g.103422194A>G GRCh37
NC_000004.10:g.103641226A>G NCBI36
NG_050628.1:g.4709A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+212T>C XP_011530769.1:n.643+212T>C
NR_136202.1:n.48+1402T>C
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